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Two-electron reduction of penta(organo)[60]fullerenes C(60)Ar(5)H (Ar = Ph and biphenyl) by potassium/mercury amalgam afforded potassium complexes of the corresponding open-shell radical dianions [K+(thf)n]2[C60Ar5(2-.)]. These compounds were characterized by UV-visible-near-IR and electron spin
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In this article we present preliminary results of the application of potassium cationized field desorption mass spectrometry as an additional technique for the elucidation of structure and evaluation of purity of oligopeptides such as C-terminal penta- and hexapeptide analogs of substance P. In the
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The title arsenatomolybdate, K(5)[Mo(8)O(24)(OH)(2)(AsO(4))]·2H(2)O, which was obtained hydro-thermally, features an [AsMo(8)O(28)(OH)(2)](5-) anion, which is formed by two Mo(4)O(14)(OH) units that are linked by As in a sandwich-like fashion. The overall symmetry of the anion is m2m. The
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The structure of the title compound, NaK(5)Ni(5)(P(2)O(7))(4), is characterized by the presence of two crystallographically independent P(2)O(7) groups with different conformations. The conformation of the first P(2)O(7) group is eclipsed, whereas that of the second is staggered. All atoms are in
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The title compound, K[B(5)O(7)(OH)(2)], was obtained from a hydro-thermal reaction. The structure is composed of one K(+) cation and a polyborate (1) (∞)[B(5)O(7)(OH)(2)](-) anion, which consists of two six-membered rings linked by a common BO(4) tetra-hedron. The [B(5)O(7)(OH)(2)](-) units are
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The title compound, K(5)EuLi(2)F(10), belongs to so-called self-activated materials containing lanthanoid ions within the matrix. A common feature of these systems is a large separation between the closest lanthanoid ions, which is one of the crucial factors governing the self-quenching of
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The crystal structure of K(5)PrLi(2)F(10) is isotypic with those of other K(5)RELi(2)F(10) compounds (RE = Eu, Nd). The lanthanoid ions are isolated in K(5)PrLi(2)F(10), with a mean separation between the Pr ions of 7.356 Å. It classifies this crystal as a so-called self-activated material
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The title compound, K5[H2PtV9O28]·9H2O, containing the nona-vanado-platinate(IV) polyanion, was obtained by hydro-thermal reaction at pH = 4.2. The polyanion has approximate mm2 (C 2v ) symmetry. The two platinum-bound μ2-O atoms are protonated in the polyanion. The heteropolyanions form
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The title compound, K11[α-Pt(μ3-OH)2(μ3-OH0.5)Mo6(μ3-O)3(μ2-O)6O12]2·12H2O (simplified chemical formula K11[H2.5PtMo6O24]2·12H2O), containing the well-known Anderson-type heteropolyoxomolybdate anion, was obtained by hydro-thermal reaction at pH = ca 6.0. The complete polyanion dimer has 2/m
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Microperoxidase 8 (MP8), a heme octapeptide obtained by hydrolytic digestion of cytochrome c, was adsorbed at the surface of a roughened silver electrode in order to provide a new supported biomimetic system for hemoproteins. A combination of two techniques was used to study its redox and
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